Carullo Nazareno, Sorbo David, Faga Teresa, Pugliese Sara, Zicarelli Maria Teresa, Costa Davide, Ielapi Nicola, Battaglia Yuri, Pisani Antonio, Coppolino Giuseppe, Bolignano Davide, Michael Ashour, Serra Raffaele, Andreucci Michele
"G. Jazzolino" Hospital, A.S.P. Vibo Valentia, I89900 Vibo Valentia, Italy.
San Bortolo Hospital, ULSS 8 Berica, I36100 Vicenza, Italy.
Int J Mol Sci. 2024 Nov 29;25(23):12838. doi: 10.3390/ijms252312838.
Anemia and mineral and bone disorder (MBD) are significant complications of chronic kidney disease (CKD). The erythropoietin (Epo) pathway plays a key role in both of these processes in CKD. Another molecule that plays an important role in CKD-MBD is fibroblast growth factor (FGF)-23, whose main role is to maintain serum phosphate levels in the normal range, acting via its co-receptor Klotho; however, its activity may also be related to anemia and inflammation. In this review, the regulation of Epo and FGF-23 and the molecular mechanisms of their action are outlined. Furthermore, the complex interaction between EPO and FGF-23 is discussed, as well as their association with other anemia-related factors and processes such as Klotho, vitamin D, and iron deficiency. Together, these may be part of a "kidney-bone marrow-bone axis" that promotes CKD-MBD.
贫血以及矿物质与骨代谢紊乱(MBD)是慢性肾脏病(CKD)的重要并发症。促红细胞生成素(Epo)途径在CKD的这两个过程中均起着关键作用。另一种在CKD-MBD中发挥重要作用的分子是成纤维细胞生长因子(FGF)-23,其主要作用是通过其共受体Klotho将血清磷酸盐水平维持在正常范围内;然而,其活性也可能与贫血和炎症有关。在本综述中,概述了Epo和FGF-23的调节及其作用的分子机制。此外,还讨论了EPO与FGF-23之间的复杂相互作用,以及它们与其他贫血相关因素和过程(如Klotho、维生素D和缺铁)的关联。这些因素共同作用,可能构成促进CKD-MBD的“肾-骨髓-骨轴”的一部分。